FDA Regulation of GMO Labeling

Pre Recorded | Best Sellers

  • 60 minutes

View the latest Press release and more!

A genetically modified organism, or GMO, is an organism that has had its DNA altered or modified in some way through genetic engineering. According to the National Library of Medicine (NLM), genetically engineered foods have had foreign genes (genes from other plants or animals) inserted into their genetic codes. The potential benefits are foods that are tastier, more nutritious and resistant to diseases and droughts. By far the biggest use of GMO technology has been in large-scale agricultural crops. If there is a meaningful difference in the safety, composition or nutrition of the crop from which the ingredients were derived, the FDA could require additional information be added to the label.  

This webinar with expert Norma Skolnik will provide an overview of the status of GMO’s in the USA and FDA’s position on GMO’s and GMO labeling. It will also cover state initiatives re: GMO labeling, worldwide GMO labeling regulations, and the various legislation that has been introduced into the U.S. Congress and passed regarding GMO labeling requirements.

Session Highlights: 

  • Status of GMO’s in the USA

  • FDA Position on GMO’s/GE foods

  • FDA Biotechnology Policy & Consultation Program

  • Worldwide GMO Labeling Regulations

  • State Initiatives & Vermont Law re: GMO Labeling

  • HR 1599: Proposed Bill to Override State Labeling Laws

  • July 2016 Compromise GMO Labeling Bill  

Who Should Attend:

  • Regulatory Managers, Associates, and Coordinators

  • Directors of Regulatory Affairs

  • Labeling managers

  • Product managers

  • Quality Managers

  • QA directors

  • Food marketing managers

  • Food industry companies

  • Consumer products companies

  • Food packaging industry representatives

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Norma Skolnik

Norma Skolnik

Norma Skolnik is currently a Regulatory Consultant with over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She was Director of Regulatory Affairs for the Americas for Cadbury Adams and Director of Regulatory Affairs for the Adams division of Pfizer before that. Prior to that she was Associate Director of Regulatory Affairs for the Warner-Lambert company and Associate Director Regulatory Affairs at American Home Products Whitehall-Robbins Division.

Quality Compliance Specialist


Information was good at times and presentation was good to follow.

by Cody Ebert, Belmark Inc

FDA Regulation of GMO Labeling by NORMA SKOLNIK


It would be nice to be able to address both FDA and USDA in terms of what will be expected in the labeling come July 2018 with some examples.

by Richard Young

Want to attend in a Group? Call 844-810-1151 and Save upto 50%

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  • $164.00

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